MICROWAVE-ASSISTED SOLVENT-FREE ARYLATION OF AMINO ACIDS WITH HALOGENOBENZENES

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dc.contributor.authorSowole, M.A.
dc.contributor.authorAdebisi, A.B.
dc.contributor.authorOlasupo, I.A.
dc.contributor.authorIzunobi, J.U.
dc.contributor.authorFamiloni, O.B.
dc.date.accessioned2019-09-05T09:57:24Z
dc.date.available2019-09-05T09:57:24Z
dc.date.issued2018-06-21
dc.description.abstractThe solventless microwave-assisted arylation and heteroarylation of different aliphatic and cyclic amino acids 2a–e were carried out on activated, substituted o-nitrohalogenobenzenes 1a–h and 2-chloro-3-nitropyridine 1i, in the presence of potassium carbonate and potassium fluoride for 0.5 h at 70 W, to give substituted N-(o-nitrophenyl)amino-2-carboxylic acid 3–16 and N-(m-nitropyridyl)amino-2-carboxylic acid 17–18 adducts in yields ranging from 5–98% .en_US
dc.identifier.citationSowole, M. A., Adebisi, A. B., Olasupo, I. A., Izunobi, J. U., & Familoni, O. B. (2018). Microwave-Assisted Solvent-Free Arylation of Amino acids with Halogenobenzenes. Journal of Chemical Society of Nigeria, 43(3).en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/5166
dc.language.isoen_USen_US
dc.publisherjournals.chemsociety.org.ngen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistryen_US
dc.subjectamino acidsen_US
dc.subjectarylationen_US
dc.subjecthalogenobenzenesen_US
dc.subjectmicrowave synthesisen_US
dc.titleMICROWAVE-ASSISTED SOLVENT-FREE ARYLATION OF AMINO ACIDS WITH HALOGENOBENZENESen_US
dc.typeArticleen_US
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